GInPipe
GInPipe estimates SARS-CoV-2 infection incidence from viral genome sequences to reconstruct temporal transmission dynamics and account for biases introduced by variable testing policies.
Key Features:
- Genome-Based Estimation: Uses SARS-CoV-2 genomic data to estimate infection incidence independently of reported case counts.
- Bias Mitigation: Mitigates biases introduced by varying national testing policies that affect detection and reporting of cases.
- Phylodynamic Independence: Reconstructs pandemic waves without requiring complex phylodynamic reconstructions.
- Rapid Execution: Executes within minutes on very large datasets, enabling near real-time analysis.
Scientific Applications:
- Incidence Reconstruction: Reconstructs incidence histories from viral sequences for regions such as Denmark, Scotland, Switzerland, and Victoria (Australia).
- Policy Evaluation: Assesses how different testing policies influence the probability of diagnosing and reporting infections and identified periods of significant under-reporting in mid-2020 across several countries.
- Pandemic Monitoring: Provides a genome-based perspective to complement surveillance tools and inform public-health understanding of SARS-CoV-2 spread.
Methodology:
Validated against simulated outbreak data and compared with more complex phylodynamic analyses to ensure accurate reconstruction of incidence dynamics from viral sequence data alone.
Topics
Collections
Details
- License:
- GPL-3.0
- Tool Type:
- workflow
- Programming Languages:
- Python, R
- Added:
- 9/20/2021
- Last Updated:
- 9/20/2021
Operations
Publications
Smith MR, Trofimova M, Weber A, Duport Y, Kühnert D, von Kleist M. Rapid incidence estimation from SARS-CoV-2 genomes reveals decreased case detection in Europe during summer 2020. Unknown Journal. 2021. doi:10.1101/2021.05.14.21257234.
Links
Issue tracker
https://github.com/KleistLab/GInPipe/issues